510(k) K112844
K112844 is an FDA 510(k) premarket notification submitted by Hasomed GmbH for the device "REHASTIM 2, REHAMOVE 2". The FDA issued a decision of Substantially Equivalent on Oct 27, 2011. The device falls under product code GZI (Stimulator, Neuromuscular, External Functional), a Class II device regulated under 21 CFR 882.5810. Hasomed GmbH has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 27, 2011
- Date Received
- Sep 29, 2011
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Neuromuscular, External Functional
- Device Class
- Class II
- Regulation Number
- 882.5810
- Review Panel
- NE
- Submission Type
- 510(k)